HAND SANITIZER- alcohol gel 
CDMA

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Quality Choice Advanced Hand Sanitizer with Aloe
439.001/439AC rev 1

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable. Keep away from heat and flame.

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

water, aloe barbadensis leaf juice,glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

Questions?

1-888-593-0593

**Effective at eliminating more than 99.99% of many comon harmful germs and bacteria in as little as 15 seconds

Distributed by CDMA, Inc.

43157 W Nine Mile

Novi, MI 48376

www.qualitychoice.com

Questions 800-935-2362

principal display panel

QC QUALITY CHOICE

Compare to Germ-X Advanced Hand Sanitizer with Aloe

Advanced

Hand Sanitizer

With Aloe

Kills More Than 99.99% of Germs*

Leaves hands feeling soft

With Moisturizer & Vitamin E

8 FL OZ (236 mL)

image description

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-439
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SULISOBENZONE (UNII: 1W6L629B4K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-439-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/05/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/05/2021
Labeler - CDMA (011920774)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(63868-439)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(63868-439)

Revised: 3/2022
Document Id: 8e08a0dc-d9d0-462e-81bf-e9dd8d821541
Set id: ac0e1491-aa50-4dbb-ae84-f50bda3fb37c
Version: 6
Effective Time: 20220303
 
CDMA